Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Facies (D019066)
Parent Node: Growth Disorders (D006130)
Parent Node: Malocclusion (D008310)
..Starting node ..Malocclusion and Short Stature (C565421)
Child Nodes:
Sister Nodes:
..Dental Occlusion, Traumatic (D003769)
..Diastema (D003970) 1
..Malocclusion and Short Stature (C565421)
..Malocclusion, Angle Class I (D008311)
..Malocclusion, Angle Class II (D008312) 1
..Malocclusion, Angle Class III (D008313)
..Open Bite (D024343)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6748
Name:	Malocclusion and Short Stature
Definition:
Alternative IDs:
ParentIDs:	MESH:D006130\|MESH:D008310\|MESH:D019066
TreeNumbers:	C07.793.494/C565421 \|C23.550.291.812/C565421 \|C23.550.393/C565421
Synonyms:
Slim Mappings:	Mouth disease\|Pathology (process)
Reference:	MedGen: C565421 MeSH: C565421 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants